HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484350Generated: October 30, 2026
Ammonium Chloride → HCID 20084230, compound
https://huagongshe.com/reaction/484350
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Trimethylsilyl isocyanate | HCID 70696 | — |
| Reactant | HCID 20084229 | HCID 20084229 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 20084230 | HCID 20084230 | — |
Reaction Steps
0.94 g (8.13 mmol) of trimethylsilyl isocyanate is added dropwise under an argon atmosphere at room temperature to a solution of 2.7 g (7.45 mmol) of N-[4-(quinolin-2-yl-methoxy)phenyl-cyclohexyl]methyl-hydroxylamine in 25 ml of dioxane p.a. The reaction mixture is heated at 100° C. under an argon atmosphere for 2.5 h, cooled to room temperature and treated with saturated ammonium chloride solution. It is extracted several times with ether, and the organic phase is dried over sodium sulphate and concentrated in vacuo. The product is obtained after column chromatography on silica gel using dichloromethane/methanol (9:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05231103 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-a17cfa0e25de4db8b9df325a3f55bbbe |
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| Source note | uspto-grants-1993_07 |
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